Department of Metabolism and Nutrition, Institute of Food Science and Technology and Nutrition (ICTAN), Consejo Superior de Investigaciones Científicas (CSIC), José Antonio Novais 10, Ciudad Universitaria, Madrid, Spain.
Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), ISCIII, Spain.
Mol Nutr Food Res. 2018 Feb;62(4). doi: 10.1002/mnfr.201700470. Epub 2018 Jan 12.
(-)-Epicatechin (EC) and main colonic phenolic acids derived from flavonoid intake, such as 2,3-dihydroxybenzoic acid (DHBA), 3,4-dihydroxyphenylacetic acid (DHPAA), 3-hydroxyphenylpropionic acid (HPPA), and vanillic acid (VA), have been suggested to exert beneficial effects in diabetes, although the mechanism for their actions remains unknown. In this study, the modulation of glucose homeostasis and insulin signaling by the mentioned compounds on renal proximal tubular NRK-52E cells is investigated.
Levels of the glucose transporters SGLT-2 and GLUT-2, as well as glucose uptake, glucose production, and key proteins of the insulin pathways, namely insulin receptor (IR), insulin receptor substrate-1 (IRS-1), and PI3K/AKT pathway are analyzed. EC (5-20 μm) and DHBA (20 μm) reduced both renal glucose uptake and production. Interestingly, EC and DHBA did not modify the levels of SGLT-2 and GLUT-2, and modulated the expression of phosphoenolpyruvate carboxykinase via AKT leading to a diminished glucose production. EC and DHBA also enhanced the tyrosine phosphorylation and total IR and IRS-1 levels, and activated the PI3K/AKT pathway in NRK-52E cells.
EC and DHBA regulate the renal glucose homeostasis by modulating both glucose uptake and production, and strengthen the insulin signaling by activating key proteins of that pathway in NRK-52E cells.
(-)-表儿茶素(EC)和主要来源于黄酮类化合物摄入的结肠酚酸,如 2,3-二羟基苯甲酸(DHBA)、3,4-二羟基苯乙酸(DHPAA)、3-羟基苯丙酸(HPPA)和香草酸(VA),被认为对糖尿病有有益的影响,尽管其作用机制尚不清楚。在这项研究中,研究了上述化合物对肾近端小管 NRK-52E 细胞葡萄糖稳态和胰岛素信号的调节作用。
分析了葡萄糖转运体 SGLT-2 和 GLUT-2 的水平,以及葡萄糖摄取、葡萄糖产生和胰岛素途径的关键蛋白,即胰岛素受体(IR)、胰岛素受体底物-1(IRS-1)和 PI3K/AKT 途径。EC(5-20 μm)和 DHBA(20 μm)降低了肾葡萄糖摄取和产生。有趣的是,EC 和 DHBA 并没有改变 SGLT-2 和 GLUT-2 的水平,而是通过 AKT 调节磷酸烯醇丙酮酸羧激酶的表达,导致葡萄糖产生减少。EC 和 DHBA 还增强了 NRK-52E 细胞中酪氨酸磷酸化和总 IR 和 IRS-1 水平,并激活了 PI3K/AKT 途径。
EC 和 DHBA 通过调节葡萄糖摄取和产生来调节肾葡萄糖稳态,并通过激活该途径的关键蛋白来增强 NRK-52E 细胞中的胰岛素信号。